Canonical Allele Identifier: CA633478855

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1250149057
• gnomAD v2: 19-45452224-G-GC
• gnomAD v3: 19-44948967-G-GC
• gnomAD v4: 19-44948967-G-GC
• MyVariant Identifiers: chr19:g.45452224_45452225insC (hg19) ; chr19:g.44948967_44948968insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948969dup , CM000681.2:g.44948969dup	GRCh38
NC_000019.9:g.45452226dup , CM000681.1:g.45452226dup	GRCh37
NC_000019.8:g.50144066dup	NCBI36
NG_008837.1:g.7984dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+109dup (APOC2) MANE Select	ENSP00000252490.5:n.215+109dup
ENST00000252490.5:c.215+109dup (APOC4-APOC2)	ENSP00000252490.4:n.215+109dup
ENST00000585685.5:c.*998+109dup (APOC4-APOC2)	ENSP00000467185.1:n.*998+109dup
ENST00000585786.1:c.*105dup (APOC2)	ENSP00000465001.1:n.*105dup
ENST00000589057.5:c.446+109dup (APOC4-APOC2)	ENSP00000468139.1:n.446+109dup
ENST00000590360.2:c.215+109dup (APOC2)	ENSP00000466775.1:n.215+109dup
ENST00000591597.5:c.173+151dup (APOC2)	ENSP00000476835.1:n.173+151dup
ENST00000592257.5:c.*9+109dup (APOC2)	ENSP00000477261.1:n.*9+109dup
NM_000483.4:c.215+109dup (APOC2)	NP_000474.2:n.215+109dup
NR_037932.1:n.1422+109dup (APOC4-APOC2)
NM_000483.5:c.215+109dup (APOC2) MANE Select	NP_000474.2:n.215+109dup